c-glycosylflavones from the leaves of iris tectorum maxim.
Clicks: 81
ID: 204604
2012
Article Quality & Performance Metrics
Overall Quality
Not rated
Combines reader engagement with the AI quality analysis. This
article has not been analysed, so there is no overall score —
reader engagement is measured and shown alongside.
Reader Engagement
Popular Article
24.0
/100
81 views
24 readers
AI Quality Assessment
Not analyzed
Readership in this journal
PopularRanked #81 of 88 articles by views in energy policy
Most read
Least read
Bar heights use a square-root scale.
Mint this article as an NFT
Not yet mintedCreate a permanent, verifiable on-chain record of this article on the Scimatic Network. The NFT is held in your Journament account, and you can withdraw it to your own wallet at any time.
5
SUSD
one-off · no wallet required
Abstract
A new C-glycosylflavone, 5-hydroxyl-4′,7-dimethoxyflavone-6-C-[O-(α-l-3′′′-acetylrhamnopyranosyl)-1→2-β-d-glucopyranoside] (1), along with five known C-glycosylflavones, 5-hydroxy-4′,7-dimethoxyflavone-6-C-[O-(α-l-2′′′-acetylrhamnopyranosyl)-1→2-β-d-glucopyranoside] (2), embinin (3), embigenin (4), swertisin (5) and swertiajaponin (6) were isolated from the leaves of Iris tectorum Maxim. Their structures were elucidated on the basis of extensive NMR experiments and spectral methods and their cytotoxic activities against A549 (lung cancer) human cell lines were determined.
| Reference Key |
ma2012actac-glycosylflavones
Use this key to autocite in the manuscript while using
SciMatic Manuscript Manager or Thesis Manager
|
|---|---|
| Authors | ;Yuhan Ma;Huan Li;Binbin Lin;Guokai Wang;Minjian Qin |
| Journal | energy policy |
| Year | 2012 |
| DOI |
10.1016/j.apsb.2012.10.007
|
| URL | |
| Keywords |
Citations
No citations found. To add a citation, contact the admin at info@scimatic.org
Comments
No comments yet. Be the first to comment on this article.